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        JPA Prize in 2014

        2015-11-17 01:24:02
        Journal of Pharmaceutical Analysis 2015年4期

        JPA Prize in 2014

        The outstanding editor awarded the 2014 JPA Prize was as follows:

        Bart De Spiegeleer

        Department of Pharmaceutical Analysis

        Drug Quality & Registration group

        Ghent University

        Belgium

        The two excellent referees awarded the 2014 JPA Prize were as follows:

        1. Stacy Brown

        Pharmaceutical Sciences

        East Tennessee State University

        United States of America

        2. Satyanarayanaraju Sagi

        School of Pharmacy

        National Center for Natural Products Research

        University of Mississippi

        United States of America

        The three top cited papers awarded the 2014 JPA Prize were as follows:

        1. Joseph J. Kirkland, Stephanie A. Schuster*, William L. Johnson, Barry E. Boyes. Fused-core particle technology in high-performance liquid chromatography: An overview. Journal of Pharmaceutical Analysis, 2013, 3(5): 303-312.

        2. Srinivasa Rao Polagani, Nageswara Rao Pilli,Ramakrishna Gajula, Venkateswarlu Gandu*.

        Simultaneous determination of atorvastatin, metformin and glimepiride in human plasma by LC-MS/MS and its application to a human pharmacokinetic study. Journal of Pharmaceutical Analysis, 2013, 3(1): 9-19.

        3. T. Satyanarayana Raju*, O. Vishweshwari Kutty,V. Ganesh, P. Yadagiri Swamy. A validated stabilityindica

        ting LC method for the separation of enantiomer and potential impurities of Linezolid using polar organic mode. Journal of Pharmaceutical Analysis, 2012, 2(4): 272-278.

        JPA Prize Medal

        Fig. 2 Separation of anticoagulants with fused-core columns of different selectivities. Columns: 50 mm × 4.6 mm Halo C18, 50 mm × 4.6 mm Halo RP-amide, 50 mm × 4.6 mm Halo phenyl-hexyl; mobile phase: A/B = 40/60; A = 0.1% formic acid, pH 2.6; B = methanol/acetonitrile,50/50; flowrate: 2.0 mL/min; temperature: 45 oC; pressure: 210 bar;detector, UV: 254 nm; 1 μL injection; andsolutes: (1) uracil, (2)4-hydroxycoumarin, (3) coumarin, (4) 6-chloro-4-hydroxycoumarin, (5)warfarin, (6) coumatetralyl, and (7) coumachlor, i = impurity.

        Fig. 3 Complete degradation profile of Linezolid along with the % impurity formation and corresponding mass nos. of impurities.

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